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Clinical Research on Nonalcoholic Fatty Liver Disease

Clinical Research on Nonalcoholic Fatty Liver Disease
非酒精性脂肪肝的临床研究
批准号:
10666491
负责人:
ROHIT LOOMBA
金额:
$97.47万
依托单位国家:
美国
项目类别:
财政年份:
2002
资助国家:
美国
项目状态:
已结题
起止时间:
2002-09-15 至 2024-06-30
关键词:
Academic Medical CentersAddressAdolescentAdultAffectAncillary StudyCaliforniaCardiovascular systemChildChildhoodCirrhosisClinicalClinical Course of DiseaseClinical ResearchClinical TrialsCurcuminData Coordinating CenterDatabasesDevelopmentDiagnosisDiagnosticDiseaseDisease ProgressionDisease modelEnrollmentEnvironmental Risk FactorFibrosisFundingFutureGeneticHepatocyteHeritabilityHistologicHistologyImageIndividualInflammationKnowledgeLeadLeadershipLife StyleLinkLiverLobularLosartanMalignant NeoplasmsMalignant neoplasm of liverMeasuresMedicineMethodsMinorityMonitorNational Institute of Diabetes and Digestive and Kidney DiseasesNatural HistoryNuclear Hormone ReceptorsOralOutcomeParentsParticipantPathogenesisPediatricsPerformancePhasePhenotypePlacebosPlayPredispositionPrognosisProteomicsPublishingRadiology SpecialtyReagentRegistriesResearchResearch PersonnelRiskRoleSerum ProteinsSiteTechnologyTherapeutic Clinical TrialTranslational ResearchUnited StatesUniversitiesValidationVariantWorkaptamerbioimagingcell injurychronic liver diseaseclinical centerclinical data repositoryclinical developmentclinical materialcohortdesigndiagnostic biomarkerdisorder preventioneffective therapygenetic variantgut microbiomeimaging modalityimprovedinnovationliver transplantationlongitudinal databasemembermortalitynon-alcoholic fatty liver diseasenonalcoholic steatohepatitisnoninvasive diagnosisnovelpediatric non-alcoholic fatty liver diseasepredictive markerpreventpublic-private partnershiprandomized, clinical trialsrecruitrepositorysafety assessmenttranslational studytreatment responsetreatment strategy

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Project Summary/Abstract The Nonalcoholic Steatohepatitis Clinical Research Network (NASH CRN) at Columbia University and its subcontracted sites at the University of California, San Diego have played a major role over the past 16 years in furthering the understanding of nonalcoholic fatty liver disease in children and adults. Given that NAFLD is the most common chronic liver disease in the United States and that known outcomes include cirrhosis, liver transplant and liver cancer, it is imperative that we develop better noninvasive measures to diagnose with more severe or progressive forms of NAFLD and that we find improved therapies with unique and rational targets. The proposal in this limited competition renewal for our Clinical Center demonstrates the progress made in longitudinal database studies and significant findings in past and current/ongoing randomized clinical trials in adults and children. Our Center and the Network describe plans for completion and continued development of clinical trials, for finding novel bio-imaging methods to assess response to therapy, to define and evaluate the performance of imaging as a noninvasive marker that might be used as a surrogate for certain features of NAFLD/NASH and as a means of tracking disease progression and to complete and develop ancillary studies for understanding the role of genetic and environmental factors in modulating the course of disease. In this regard, we lead studies in developing proteomic reagents as predictive and diagnostic markers for NAFLD; in elucidating the role of the gut microbiome, the role of nuclear hormone receptors, and the role of genetic variants in pediatric NAFLD. We intend to continue to play leading roles in the NASH CRN, as the PI is Co-Chair of the Steering Committee and Database Committee, a member of the Executive Committee, and Chair of the Pediatric Committee. Our Centers’ leading role in enrollment, along with our leadership in recruitment and retention of adults, children and minorities in the NASH CRN are expected to continue through completion of current trials and initiation of newly proposed studies.
期刊论文(127)
专著(0)
科研奖励(0)
会议论文
DOI: 10.1080/19490976.2024.2304157
发表时间: 2024-01
期刊: Gut microbes
影响因子: 12.2
作者: []
通讯作者:
DOI: 10.1053/j.gastro.2021.10.051
发表时间: 2022-03
期刊: Gastroenterology
影响因子: 29.4
作者: [Loomba R, Ratziu V, Harrison SA, NASH Clinical Trial Design International Working Group]
通讯作者: NASH Clinical Trial Design International Working Group
DOI: 10.1007/s11938-020-00290-2
发表时间: 2020-06
期刊: Current treatment options in gastroenterology
影响因子: --
作者: [Mouzaki M, Loomba R]
通讯作者: Loomba R
DOI: 10.1136/gutjnl-2021-324264
发表时间: 2022-05
期刊: Gut
影响因子: 24.5
作者: [Tamaki N, Munaganuru N, Jung J, Yonan AQ, Loomba RR, Bettencourt R, Ajmera V, Valasek MA, Behling C, Sirlin CB, Loomba R]
通讯作者: Loomba R
87
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    San Diego Cirrhosis Clinical Research Network
    Role of liver fat and fibrosis in human CVD risk phenotypes.
    Role of liver fat and fibrosis in human CVD risk phenotypes.
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